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Showing 141–150 of 68654 articles for “Art. L. 123-11 and L. 123-11-1”
…he holder of the parallel import authorisation is responsible for placing the product on the market and, in this capacity, ensures that the provisions of this Title are complied with, in particular th…
…of the parallel import authorisation in the summary of product characteristics, the package leaflet and the labelling of the proprietary veterinary medicinal product as marketed in France.
…ite of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail.
I.- In the event of repackaging, the holder of a parallel import authorisation for a proprietary veterinary medicinal product shall notify the holder of the marketing authorisation for the proprietary…
The holder of a parallel import authorisation for a proprietary veterinary medicinal product shall immediately inform the marketing authorisation holder in the country of origin of any serious adverse…
The administrative authority referred to in articles L. 1237-19-3 to L. 1237-19-5, L. 1237-19-7 and L. 1237-19-8 is the regional director of companies, competition, consumption, labour and employment…
…veterinary medicinal product which has already been the subject of a parallel import authorisation, and the proprietary veterinary medicinal product which is the subject of the application comes from…
…by the same company or by an associated company or working under licence with the same quantitative and qualitative composition in active ingredients and excipients and the same pharmaceutical form as…
The copy of the import authorisation or temporary use authorisation referred to in article L. 5141-10 is presented during the inspection by the customs officers. For imported veterinary medicinal prod…
…imentation, de l'environnement et du travail must indicate : 1° The name or corporate name, address and position of the natural or legal person responsible for the import ; 2° The country of origin an…
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